Earlywood vessels of the sub-Mediterranean oak Quercus pyrenaica have greater plasticity and sensitivity than those of the temperate Q. petraea at the Atlantic–Mediterranean boundary
- 458 Downloads
- 20 Citations
Abstract
Key message
Earlywood vessel features indicate different adaptations of Quercus petraea and Q. pyrenaica , which are probably related with their corresponding Atlantic and sub-Mediterranean ecological requirements.
Abstract
We studied the climatic signal of the earlywood anatomy of a temperate [Quercus petraea (Mattuschka) Liebl.] and a sub-Mediterranean (Quercus pyrenaica Willd.) oak species growing under similar climatic conditions in a transitional area between the Atlantic and Mediterranean regions of the Iberian Peninsula. We hypothesized that both species react differently in their wood anatomy due to their contrasting ecological requirements, and we test the usefulness of earlywood anatomical features to study the behaviour of these ring-porous oaks upon climate. For this, we measured the earlywood vessels, and obtained annual series of several anatomical variables for the period 1937–2006 using dendrochronological techniques, considering whether the vessels belonged to the first row or not. After optimizing the data set by principal component analysis and progressive filtering of large vessels, we selected maximum vessel area and total number of vessels as they resulted to be the optimal variables to describe vessel size and number, respectively. Vessel size of Q. pyrenaica was dependent on precipitation along the previous growing season, whereas it did not show any clear climatic response for Q. petraea. On the contrary, vessel number was related to winter temperature for both species. These relationships observed between climate and anatomy appeared to be stable through time. The results obtained reinforce the utility of earlywood vessel features as potential climate proxies.
Keywords
Climatic signal Tree ring Dendrochronology Wood anatomy Vessel sizeNotes
Acknowledgments
We thank Sabrina Aldao and Adrián González for field and laboratory assistance, and the Servicio de Montes y Conservación de la Naturaleza de Cantabria for permission for coring trees in Monte Hijedo Natural Park. Rosa Ana Vázquez commented on an earlier version of his manuscript. B. D. González-González benefited from Maria Barbeito pre-doctoral fellowship by Galicia Government. V. Rozas benefited from research contracts by INIA-Xunta de Galicia and CSIC. This research was funded by Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Spanish Ministry of Science and Innovation (RTA2006-00117). We are also grateful to two anonymous reviewers for their useful suggestions.
References
- Alcamo J, Moreno JM, Nováky B, Bindi M, Corobov R, Devoy R (2007) Europe: impacts, adaptation and vulnerability. Contribution of Working Group II to the fourth assessment report of the Intergovernmental Panel on Climate Change. Cambridge University Press, Cambridge, pp 541–580Google Scholar
- Barbaroux C, Bréda N (2002) Contrasting distribution and seasonal dynamics of carbohydrate reserves in stem wood of adult ring-porous sessile oak and diffuse-porous beech trees. Tree Physiol 22:1201–1210PubMedCrossRefGoogle Scholar
- Benito-Garzón M, Sánchez-DeDios R, Sainz-Ollero H (2008) Effects of climate change on the distribution of Iberian tree species. Appl Veg Sci 10:877–885Google Scholar
- Biondi F (1997) Evolutionary and moving response functions in dendroclimatology. Dendrochronologia 15:139–150Google Scholar
- Bradley NL, Leopold AC, Ross J, Huffaker W (1999) Phenological changes reflect climate change in Wisconsin. Proc Natl Acad Sci USA 96:9701–9704PubMedCrossRefGoogle Scholar
- Bréda N, Granier A (1996) Intra and interannual variations of transpiration, leaf area index and radial growth of a sessile oak (Quercus petraea). Ann For Sci 53:521–536CrossRefGoogle Scholar
- Briffa K, Jones PD (1992) Basic chronology statistics and assessment. In: Cook ER, Kairiukštis LA (eds) Methods of dendrochronology. Applications in the environmental sciences. Kluwer, Boston, pp 137–153Google Scholar
- Briffa KR, Osborn T, Schweingruber F (2004) Large-scale temperature inferences from tree rings. Global Planet Change 40:11–26CrossRefGoogle Scholar
- Bryukhanova M, Fonti P (2013) Xylem plasticity allows rapid hydraulic adjustment to annual climatic variability. Trees 27:485–496CrossRefGoogle Scholar
- Büntgen U, Frank D, Schmidhalter M, Neuwirth B, Seifert M, Esper J (2006) Growth/climate responses shift in a long subalpine spruce chronology. Trees 20:99–110CrossRefGoogle Scholar
- Campelo F, Nabais C, Gutiérrez E, Freitas H, García-González I (2010) Vessel features of Quercus ilex L. growing under Mediterranean climate have a better climatic signal than tree-ring width. Trees 24:463–470CrossRefGoogle Scholar
- Christman MA, Sperry JS, Smith DD (2012) Rare pits, large vessels and extreme vulnerability to cavitation in a ring-porous tree species. New Phytol 193:713–720PubMedCrossRefGoogle Scholar
- Cook ER (1992) A conceptual linear aggregate model for tree rings. In: Cook ER, Kairiukštis LA (eds) Methods of dendrochronology. Applications in the environmental sciences. Kluwer, Boston, pp 98–104Google Scholar
- D’Arrigo R, Wilson R, Liepert B, Cherubini P (2008) On the divergence problem in Nothern forest: a review of the tree-ring evidence and possible causes. Glob Planet Change 60:289–305CrossRefGoogle Scholar
- Eilmann B, Weber P, Rigling A, Eckstein D (2006) Growth reactions of Pinus sylvestris L. and Quercus pubescens Willd. to drought years at a xeric site in Valais, Switzerland. Dendrochronologia 23:121–132CrossRefGoogle Scholar
- Farrar JJ, Evert RF (1997) Seasonal changes in the ultrastructure of the vascular cambium of Robinia pseudoacacia. Trees 11:191–201Google Scholar
- Fonti P, García-González I (2004) Suitability of chestnut earlywood vessel chronologies for ecological studies. New Phytol 163:77–86CrossRefGoogle Scholar
- Fonti P, García-González I (2008) Earlywood vessel size of oak as potential proxy for spring precipitation in mesic sites. J Biogeogr 35:2249–2257CrossRefGoogle Scholar
- Fonti P, Solomonoff N, García-González I (2007) Earlywood vessels of Castanea sativa Mill. record temperature prior to their formation. New Phytol 173:562–570PubMedCrossRefGoogle Scholar
- Fonti P, Eilmann B, García-González I, von Arx G (2009) Expeditious building of ring-porous earlywood vessel chronologies without loosing signal information. Trees 23:665–671CrossRefGoogle Scholar
- Fonti P, von Arx G, García-González I, Eilmann B, Sass-Klaassen U, Gärtner H, Eckstein D (2010) Studying global change through investigation of the plastic responses of xylem anatomy in tree rings. New Phytol 185:42–53PubMedCrossRefGoogle Scholar
- Friedrichs DA, Büntgen U, Frank DC, Esper J, Neuwirth B, Loffler J (2009) Complex climate controls on 20th century oak growth in Central-West Germany. Tree Physiol 29:39–51PubMedCrossRefGoogle Scholar
- Fukuda H (2004) Signals that control plant vascular cell differentiation. Mol Cell Biol 5:379–391Google Scholar
- Gallé A, Haldimann P, Feller U (2007) Photosynthetic performance and water relations in young pubescent oak (Quercus pubescens) trees during drought stress and recovery. New Phytol 174:799–810PubMedCrossRefGoogle Scholar
- Gallé A, Esper J, Feller U, Ribas-Carbo M, Fonti P (2010) Responses of wood anatomy and carbon isotope composition of Quercus pubescens saplings subjected to two consecutive years of summer drought. Ann For Sci 67:809CrossRefGoogle Scholar
- García-González I, Eckstein D (2003) Climatic signal of earlywood vessels of oak on a maritime site. Tree Physiol 23:497–504CrossRefGoogle Scholar
- García-González I, Fonti P (2006) Selecting earlywood vessels to maximize their environmental signal. Tree Physiol 26:1289–1296PubMedCrossRefGoogle Scholar
- García-González I, Fonti P (2008) Ensuring a representative sample of earlywood vessels for dendroclimatological studies: an example from two ring-porous species. Trees 22:237–244CrossRefGoogle Scholar
- Gea-Izquierdo G, Fonti P, Cherubini P, Martín-Benito D, Chaar H, Canellas I (2012) Xylem hydraulic adjustment and growth response of Quercus canariensis Willd. to climatic variability. Tree Physiol 32:401–413PubMedCrossRefGoogle Scholar
- Gian-Reto W, Post E, Convey P, Menzel A, Parmesan C, Beebee TJC, Fromentin JM, Hoegh-Guldberg O, Bairlein F (2002) Ecological responses to recent climate change. Nature 416:339–395Google Scholar
- Grabherr G, Gottfried M, Pauli H (1994) Climate effects on mountain plants. Nature 369:448PubMedCrossRefGoogle Scholar
- Grissino-Mayer HD (2001) Evaluating crossdating accuracy: a manual and tutorial for the computer program Cofecha. Tree-Ring Res 57:205–221Google Scholar
- Grissino-Mayer HD (2008) A dendrochronology program library in R (dplR). Dendrochronologia 26:115–124CrossRefGoogle Scholar
- Hacke UG, Sperry JS (2001) Functional and ecological xylem anatomy. Perspect Plant Ecol Evol Syst 4:97–115CrossRefGoogle Scholar
- Hacke UG, Sperry JS, Wheeler JK, Castro L (2006) Scaling of angiosperm xylem structure with safety and efficiency. Tree Physiol 26:689–701PubMedCrossRefGoogle Scholar
- Hansen AJ, Neilson RP, Dale VH, Flather CH, Iverson LR, Currie DJ, Shafer S, Coot R, Bartlein PJ (2001) Global change in forests: responses of species, communities, and biomes. Bioscience 51:765–779CrossRefGoogle Scholar
- Hernández-Santana V, Martínez-Vilalta J, Martínez-Fernández J, Williams M (2009) Evaluating the effect of drier and warmer conditions on water use by Quercus pyrenaica. For Ecol Manage 258:1719–1730CrossRefGoogle Scholar
- Hinckley TM, Lassoie JP (1981) Radial growth in conifers and deciduous trees: a comparison. Mitt Forstl Bundesvers Wien 142:17–56Google Scholar
- Hoch G, Richter A, Körner C (2003) Non-structural carbon compounds in temperate forest trees. Plant Cell Environ 26:1067–1081CrossRefGoogle Scholar
- Lachaud S, Catesson AM, Bonnemain JL (1999) Structure and functions of the vascular cambium. C R Acad Sci III 322:633–650PubMedCrossRefGoogle Scholar
- Martínez-Vilalta J, Prat E, Oliveras I, Piñol J (2002) Hydraulic properties of roots and stems of nine woody species from a holm oak forest in NE Spain. Oecologia 133:19–29CrossRefGoogle Scholar
- Mason SJ, Mimmack GM (1992) The use of bootstrap correlation coefficients in climatology. Theor Appl Climatol 45:229–233CrossRefGoogle Scholar
- Matisons R, Brūmelis G (2012) Influence of climate on tree-ring and earlywood vessel formation in Quercus robur in Latvia. Trees 26:1251–1266CrossRefGoogle Scholar
- McDowell N, Pockman W, Allen CD, Breshears DD, Cobb N, Kolb T, Plaut J, Sperry J, West A, Williams DG, Yepez A (2008) Mechanisms of plant survival and mortality during drought: why do some plants survive while others succumb to drought? New Phytol 178:719–739PubMedCrossRefGoogle Scholar
- Mencuccini M, Martínez-Vilalta J, Piñol J, Loepfe L, Burnat M, Álvarez X, Camacho J, Gil D (2010) A quantitative and statistically robust method for the determination of xylem conduit spatial distribution. Am J Bot 97:1247–1259PubMedCrossRefGoogle Scholar
- Mérian P, Bontemps JD, Bergés L, Lebourgeois F (2011) Spatial variation and temporal instability in climate-growth relationships of sessile oak (Quercus petraea (Matt.) Liebl.) under temperate conditions. Plant Ecol 212:1855–1871CrossRefGoogle Scholar
- Michelot A, Bréda N, Damesin C, Dufrêne E (2012) Differing growth responses to climatic variations and soil water deficits of Fagus sylvatica, Quercus petraea and Pinus sylvestris in a temperate forest. For Ecol Manage 265:161–171CrossRefGoogle Scholar
- Olano JM, Eugenio M, García-Cervigón AI, Folch M, Rozas V (2012) Quantitative tracheid anatomy reveals a complex environmental control of wood structure in continental Mediterranean climate. Int J Plant Sci 173:137–149CrossRefGoogle Scholar
- Parmesan C (2006) Ecological and evolutionary responses to recent climate change. Ann Rev Ecol Evol Syst 37:637–669CrossRefGoogle Scholar
- Pop EW, Oberbauer SF, Starr G (2000) Predicting vegetative bud break in two arctic deciduous shrub species, Salix pulchra and Betula nana. Oecologia 124:176–184CrossRefGoogle Scholar
- Rasband W (2009) ImageJ. US National Institute of Health, Bethesda, Maryland, USA. http://rsb.info.nih.gov/ij. Accessed 7 March 2012
- R Development Core Team (2012) R: A language and environment for statistical computing. R Foundation for Statistical Computing, ViennaGoogle Scholar
- Sánchez-DeDios R, Benito-Garzón M, Sainz-Ollero H (2009) Present and future extension of the Iberian submediterranean territories as determined from the distribution of marcescent oaks. Plant Ecol 204:189–205CrossRefGoogle Scholar
- Sass U, Eckstein D (1995) The variability of vessel size in beech (Fagus sylvatica L.) and its ecophysiological interpretation. Trees 9:247–252CrossRefGoogle Scholar
- Schmitt U, Möller R, Eckstein D (2000) Seasonal wood formation dynamics of Beech (Fagus sylvatica L.) and Black Locust (Robinia pseudoacacia L.) as determined by the “pinning” technique. J Appl Bot 74:10–16Google Scholar
- Schume H, Grabner M, Eckmullner O (2004) The influence of an altered groundwater regime on vessel properties of hybrid poplar. Trees 18:185–194CrossRefGoogle Scholar
- Sperry JS, Meinzer FC, McCulloh KA (2008) Safety and efficiency conflicts in hydraulic architecture: scaling from tissues to trees. Plant Cell Environ 31:632–645PubMedCrossRefGoogle Scholar
- Suzuki M, Yoda K, Suzuki H (1996) Phenological comparison of the onset of vessel formation between ring-porous and diffuse-porous deciduous trees in a Japanese temperate forest. IAWA J 17:431–444Google Scholar
- Thuiller W, Lavorel S, Araújo MB, Sykes MT, Prentice IC (2005) Climate change threats to plant diversity in Europe. Proc Natl Acad Sci USA 102:8245–8250PubMedCrossRefGoogle Scholar
- Valladares F, Gianoli E, Gomez JM (2007) Ecological limits to plant phenotypic plasticity. New Phytol 176:749–763PubMedCrossRefGoogle Scholar
- Visser H, Büntgen U, D’Arrigo R, Petersen AC (2010) Detecting instabilities in tree-ring proxy calibration. Clim Past 6:367–377CrossRefGoogle Scholar
- Yang Z, Midmore DJ (2005) Modelling plant resource allocation and growth partitioning in response to environmental heterogeneity. Ecol Model 181:59–77CrossRefGoogle Scholar
- Zanne AE, Westoby M, Falster DS, Ackerly DD, Loarie SR, Arnold SEJ, Coomes DA (2010) Angiosperm wood structure: global patterns in vessel anatomy and their relation to wood density and potential conductivity. Am J Bot 97:207–215PubMedCrossRefGoogle Scholar
- Zimmermann MH (1983) Xylem structure and ascent of sap. Springer, New YorkCrossRefGoogle Scholar